law://eu/reg/2016/1930@2026-11-12THE EUROPEAN COMMISSION,Having regard to the Treaty on the Functioning of the European Union,Having regard to Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012 concerning the making available on the market and use of biocidal productsnote, and in particular the third subparagraph of Article 89(1) thereof,Whereas:
HAS ADOPTED THIS REGULATION:
| Common Name | IUPAC NameIdentification Numbers | Minimum degree of purity of the active substancenote | Date of approval | Expiry date of approval | Product type | Specific conditions |
|---|---|---|---|---|---|---|
| Chlorocresol | IUPAC Name:4-chloro-3-methylphenolEC No: 200-431-6CAS No: 59-50-7 | 99,8 % w/w | 1 May 2018 | 30 April 2028 | 1 | The authorisations of biocidal products are subject to the following condition:The product assessment shall pay particular attention to the exposures, the risks and the efficacy linked to any use covered by an application for authorisation, but not addressed in the Union-level risk assessment of the active substance. |
| 2 | The authorisations of biocidal products are subject to the following conditions:1. The product assessment shall pay particular attention to the exposures, the risks and the efficacy linked to any use covered by an application for authorisation, but not addressed in the Union-level risk assessment of the active substance.2. In view of the risks identified for the uses assessed, the product assessment shall pay particular attention to: a)industrial and professional users;b)children for products used in private and institutional areas. | |||||
| 3 | The authorisations of biocidal products are subject to the following conditions:1. The product assessment shall pay particular attention to the exposures, the risks and the efficacy linked to any use covered by an application for authorisation, but not addressed in the Union-level risk assessment of the active substance.2. In view of the risks identified for the uses assessed, the product assessment shall pay particular attention to: a)professional users;b)soil compartment.3. For products that may lead to residues in food or feed, the need to set new or to amend existing maximum residue levels (MRLs) in accordance with Regulation (EC) No 470/2009 of the European Parliament and of the Council or Regulation (EC) No 396/2005 of the European Parliament and of the Council shall be verified, and any appropriate risk mitigation measures shall be taken to ensure that the applicable MRLs are not exceeded. | |||||
| 6 | The authorisations of biocidal products are subject to the following conditions:1. The product assessment shall pay particular attention to the exposures, the risks and the efficacy linked to any use covered by an application for authorisation, but not addressed in the Union-level risk assessment of the active substance.2. In view of the risks identified for the uses assessed, the product assessment shall pay particular attention to: a)professional users during the formulation of product to be preserved and during the application of the preserved product in paper production;b)infants crawling on a surface that has been cleaned with the preserved product. | |||||
| 9 | The authorisations of biocidal products are subject to the following conditions:1. The product assessment shall pay particular attention to the exposures, the risks and the efficacy linked to any use covered by an application for authorisation, but not addressed in the Union-level risk assessment of the active substance.2. In view of the risks identified for the uses assessed, the product assessment shall pay particular attention to professional users. |
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